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Article type: Research Article
Authors: Wang, Ju; 1 | Shi, Zi-Qi; 1 | Zhang, Mu; 1 | Xin, Gui-Zhong | Pang, Tao | Zhou, Ping | Chen, Jun | Qi, Lian-Wen | Yang, Hua | Xu, Xiaojun; * | Li, Ping; *
Affiliations: State Key Laboratory of Natural Medicines, Department of Pharmacognosy, China Pharmaceutical University, Nanjing, China
Correspondence: [*] Correspondence to: Ping Li, PhD, Professor, Director, State Key Laboratory of Natural Medicines, Department of Pharmacognosy, China Pharmaceutical University; 24 Tongjia Lane, Nanjing 210009, China. Tel./Fax: +86 25 83271379; E-mail: liping2004@126.com and Xiaojun Xu, PhD, Associated Professor, State Key Laboratory of Natural Medicines, Department of Pharmacognosy, China Pharmaceutical University; 24 Tongjia Lane, Nanjing 210009, China. Tel./Fax: +86 25 83271379; E-mail: xiaojunxu2000@163.com.
Note: [1] These authors contributed equally to this work.
Abstract: Compounds derived from natural products are becoming promising alternative drugs/tools in Alzheimer's disease (AD) therapeutics. From an in-house natural products library, seventeen hits were selected for their inhibitory effect on the production of amyloid-β (Aβ) with IC50 lower than 10 μM without causing obvious toxicity. Among these compounds, camptothecin (CPT) and its analogs showed inhibitory effects on amyloid-β 1-42 (Aβ42) with the IC50 value in the nanomolar range in HEKsw cells and SHSY5Ysw cells. Further studies showed that CPT and its analogs inhibited Aβ42 via a p53 dependent pathway. Meanwhile, CPT and its analogs could also inhibit Aβ42 induced IL-1β production in the THP-1 cells. Taken together, our results indicate that CPT and its analogs would be a promising therapeutic candidates for AD.
Keywords: Alzheimer's disease, amyloid-β, camptothecin, IL-1β, p53
DOI: 10.3233/JAD-140078
Journal: Journal of Alzheimer's Disease, vol. 43, no. 2, pp. 465-477, 2015
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